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The top research priorities for congenital ichthyosis include long-term side effects of oral retinoids, best topical treatments, and treatments for itch and hair loss.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Removing a tumor may resolve associated skin and hair symptoms.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

Gluconolactone products can significantly reduce skin scaling in golden retrievers with ARCI.

Hypertrichosis (excessive hair growth) can help diagnose superficial epidermolytic ichthyosis.

Some scalp sores are linked to different inherited skin conditions.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Netherton's syndrome is linked to high IgE levels and unique skin and hair symptoms, and may improve with ammonium lactate lotion and allergy management.

Mutations in keratin genes cause cell fragility and various skin disorders.

Retinoids can help treat skin disorders by improving the skin's outer layer.

Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Over half of the dog skin disorders discussed have known gene variants, enabling genetic testing for diagnosis and responsible breeding.

In 2017, pediatric dermatology advanced with new treatments and insights into various skin conditions in children.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

A gene mutation in mice causes skin defects and early death.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Ichthyoses are skin disorders causing scales, with treatment depending on type and severity.

Many alpacas have skin diseases, with bacterial infections being the most common.

The document concludes that while finding animal models for the skin disease Hidradenitis suppurativa is challenging, certain mouse mutations may provide useful insights for research and drug testing.

Netherton Syndrome can cause severe skin lesions in rare cases.

Liquid nitrogen spray caused a temporary, harmless swelling under the skin in an elderly woman.

Topical tacalcitol ointment can help improve symptoms of EFFC.

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.